Glossary

Procedures for handling and reporting adverse events during a trial.

Research to understand how a drug is prescribed and used in the general population.

A statistical method to handle missing data in clinical trials.

The evaluation of a trial's ethical aspects to protect participant welfare.

Making clinical trial data available to researchers for further analysis.

Monitoring participants after the trial ends to assess lasting effects of a treatment.

A specific group within a trial assigned to a particular treatment or intervention.

A summary of all findings and processes at the conclusion of a clinical trial.

A study designed to evaluate the safety and efficacy of different doses of a treatment.

The group in a trial receiving a standard treatment or placebo for comparison.

A trial design allowing modifications to protocols based on interim data.

The extent to which trial results can be applied to real-world settings or populations.

An organization representing patient's interests in clinical research.

Any instance where the trial procedures are not followed as outlined in the protocol.